K241439
- 510(k) number
- K241439
- Device name
- VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage
- Applicant
- Vuno, Inc. KR
- Product code
- QFM — Radiological Computer-Assisted Prioritization Softwa
- Decision date
- 2024-11-15
- Date received
- 2024-05-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K241439.pdf
Official FDA record: K241439
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.